- Home
- Publications
- Publication Search
- Publication Details
Title
RNA toxicity in non‐coding repeat expansion disorders
Authors
Keywords
-
Journal
EMBO JOURNAL
Volume -, Issue -, Pages -
Publisher
EMBO
Online
2019-11-13
DOI
10.15252/embj.2018101112
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Sense and antisense RNA are not toxic in Drosophila models of C9orf72-associated ALS/FTD
- (2018) Thomas G. Moens et al. ACTA NEUROPATHOLOGICA
- A zebrafish model for C9orf72 ALS reveals RNA toxicity as a pathogenic mechanism
- (2018) Bart Swinnen et al. ACTA NEUROPATHOLOGICA
- Haploinsufficiency leads to neurodegeneration in C9ORF72 ALS/FTD human induced motor neurons
- (2018) Yingxiao Shi et al. NATURE MEDICINE
- C9ORF72 repeat expansion causes vulnerability of motor neurons to Ca2+-permeable AMPA receptor-mediated excitotoxicity
- (2018) Bhuvaneish T. Selvaraj et al. Nature Communications
- Small Molecules Which Improve Pathogenesis of Myotonic Dystrophy Type 1
- (2018) Marta López-Morató et al. Frontiers in Neurology
- Poly-GR dipeptide repeat polymers correlate with neurodegeneration and Clinicopathological subtypes in C9ORF72-related brain disease
- (2018) Nobutaka Sakae et al. Acta Neuropathologica Communications
- SCA8 RAN polySer protein preferentially accumulates in white matter regions and is regulated by eIF3F
- (2018) Fatma Ayhan et al. EMBO JOURNAL
- C9orf72-mediated ALS and FTD: multiple pathways to disease
- (2018) Rubika Balendra et al. Nature Reviews Neurology
- Potential pathogenic mechanisms underlying Fragile X Tremor Ataxia Syndrome: RAN translation and/or RNA gain-of-function?
- (2017) Manon Boivin et al. European Journal of Medical Genetics
- C9orf72 poly GA RAN-translated protein plays a key role in amyotrophic lateral sclerosis via aggregation and toxicity
- (2017) Youn-Bok Lee et al. HUMAN MOLECULAR GENETICS
- C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten
- (2017) Matthew J. Stopford et al. HUMAN MOLECULAR GENETICS
- Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2017) Jennifer A. Fifita et al. Neurodegenerative Diseases
- Frontotemporal Dementia
- (2017) Nicholas T. Olney et al. NEUROLOGIC CLINICS
- Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome
- (2017) Chantal Sellier et al. NEURON
- RAN Translation Regulated by Muscleblind Proteins in Myotonic Dystrophy Type 2
- (2017) Tao Zu et al. NEURON
- Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31
- (2017) Taro Ishiguro et al. NEURON
- C9orf72: At the intersection of lysosome cell biology and neurodegenerative disease
- (2017) Joseph Amick et al. TRAFFIC
- HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patients
- (2017) Wenting Guo et al. Nature Communications
- SRSF1-dependent nuclear export inhibition of C9ORF72 repeat transcripts prevents neurodegeneration and associated motor deficits
- (2017) Guillaume M. Hautbergue et al. Nature Communications
- Evidence that C9ORF72 Dipeptide Repeat Proteins Associate with U2 snRNP to Cause Mis-splicing in ALS/FTD Patients
- (2017) Shanye Yin et al. Cell Reports
- Suppression of C9orf72 RNA repeat-induced neurotoxicity by the ALS-associated RNA-binding protein Zfp106
- (2017) Barbara Celona et al. eLife
- The Role of Dipeptide Repeats in C9ORF72-Related ALS-FTD
- (2017) Brian D. Freibaum et al. Frontiers in Molecular Neuroscience
- Unraveling the Role of RNA Mediated Toxicity of C9orf72 Repeats in C9-FTD/ALS
- (2017) Vijay Kumar et al. Frontiers in Neuroscience
- Antisense Oligonucleotides Reduce RNA Foci in Spinocerebellar Ataxia 36 Patient iPSCs
- (2017) Kosuke Matsuzono et al. Molecular Therapy-Nucleic Acids
- Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 gene
- (2017) Yvonne S. Davidson et al. Acta Neuropathologica Communications
- Full ablation of C9orf72 in mice causes immune system-related pathology and neoplastic events but no motor neuron defects
- (2016) Emma Sudria-Lopez et al. ACTA NEUROPATHOLOGICA
- Repeat-associated non-AUG translation from antisense CCG repeats in fragile X tremor/ataxia syndrome
- (2016) Amy Krans et al. ANNALS OF NEUROLOGY
- The RNA binding KH domain of Spoonbill depletes pathogenic non-coding spinocerebellar ataxia 8 transcripts and suppresses neurodegeneration in Drosophila
- (2016) Bipin K. Tripathi et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin‐2 to induce motor neuron dysfunction and cell death
- (2016) Chantal Sellier et al. EMBO JOURNAL
- The C9orf72 protein interacts with Rab1a and the ULK1 complex to regulate initiation of autophagy
- (2016) Christopher P Webster et al. EMBO JOURNAL
- Reduced hnRNPA3 increases C9orf72 repeat RNA levels and dipeptide‐repeat protein deposition
- (2016) Kohji Mori et al. EMBO REPORTS
- Identification of a novel loss-of-function C9orf72 splice site mutation in a patient with amyotrophic lateral sclerosis
- (2016) Fang Liu et al. NEUROBIOLOGY OF AGING
- Gain of Toxicity from ALS/FTD-Linked Repeat Expansions in C9ORF72 Is Alleviated by Antisense Oligonucleotides Targeting GGGGCC-Containing RNAs
- (2016) Jie Jiang et al. NEURON
- C9orf72 is required for proper macrophage and microglial function in mice
- (2016) J. G. ORourke et al. SCIENCE
- Loss-of-function mutations in the C9ORF72 mouse ortholog cause fatal autoimmune disease
- (2016) Aaron Burberry et al. Science Translational Medicine
- Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy
- (2016) Fernande Freyermuth et al. Nature Communications
- Cell-to-Cell Transmission of Dipeptide Repeat Proteins Linked to C9orf72 -ALS/FTD
- (2016) Thomas Westergard et al. Cell Reports
- The C9ORF72 GGGGCC expansion forms RNA G-quadruplex inclusions and sequesters hnRNP H to disrupt splicing in ALS brains
- (2016) Erin G Conlon et al. eLife
- A C9ORF72/SMCR8-containing complex regulates ULK1 and plays a dual role in autophagy
- (2016) M. Yang et al. Science Advances
- Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD
- (2016) Michael Niblock et al. Acta Neuropathologica Communications
- Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD
- (2016) Steven Boeynaems et al. Scientific Reports
- C9orf72 ablation causes immune dysregulation characterized by leukocyte expansion, autoantibody production and glomerulonephropathy in mice
- (2016) Amanda Atanasio et al. Scientific Reports
- Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy
- (2015) Johnathan Cooper-Knock et al. ACTA NEUROPATHOLOGICA
- Cerebellar c9RAN proteins associate with clinical and neuropathological characteristics of C9ORF72 repeat expansion carriers
- (2015) Tania F. Gendron et al. ACTA NEUROPATHOLOGICA
- Quantitative analysis and clinico-pathological correlations of different dipeptide repeat protein pathologies in C9ORF72 mutation carriers
- (2015) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Novel clinical associations with specific C9ORF72 transcripts in patients with repeat expansions in C9ORF72
- (2015) Marka van Blitterswijk et al. ACTA NEUROPATHOLOGICA
- Isoform-specific antibodies reveal distinct subcellular localizations of C9orf72 in amyotrophic lateral sclerosis
- (2015) Shangxi Xiao et al. ANNALS OF NEUROLOGY
- C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits
- (2015) Max Koppers et al. ANNALS OF NEUROLOGY
- Crystallographic and Computational Analyses of AUUCU Repeating RNA That Causes Spinocerebellar Ataxia Type 10 (SCA10)
- (2015) HaJeung Park et al. BIOCHEMISTRY
- Heterozygous Deletion of KLHL1/ATX8OS at the SCA8 Locus Is Unlikely Associated With Cerebellar Impairment in Humans
- (2015) Giorgia Mandrile et al. CEREBELLUM
- Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS
- (2015) Renate K. Hukema et al. HUMAN MOLECULAR GENETICS
- RAN translation at CGG repeats induces ubiquitin proteasome system impairment in models of fragile X-associated tremor ataxia syndrome
- (2015) Seok Yoon Oh et al. HUMAN MOLECULAR GENETICS
- Nuclear accumulation of mRNAs underlies G4C2-repeat-induced translational repression in a cellular model of C9orf72 ALS
- (2015) S. Rossi et al. JOURNAL OF CELL SCIENCE
- The NF45/NF90 Heterodimer Contributes to the Biogenesis of 60S Ribosomal Subunits and Influences Nucleolar Morphology
- (2015) Franziska Wandrey et al. MOLECULAR AND CELLULAR BIOLOGY
- Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12
- (2015) Elizabeth E. O'Hearn et al. MOVEMENT DISORDERS
- The C9orf72 repeat expansion disrupts nucleocytoplasmic transport
- (2015) Ke Zhang et al. NATURE
- GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport
- (2015) Brian D. Freibaum et al. NATURE
- Distinct brain transcriptome profiles in C9orf72-associated and sporadic ALS
- (2015) Mercedes Prudencio et al. NATURE NEUROSCIENCE
- Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants
- (2015) Shahram Saberi et al. NEUROLOGIC CLINICS
- C9orf72 promoter hypermethylation is neuroprotective: Neuroimaging and neuropathologic evidence
- (2015) C. T. McMillan et al. NEUROLOGY
- C9orf72 BAC Transgenic Mice Display Typical Pathologic Features of ALS/FTD
- (2015) Jacqueline G. O’Rourke et al. NEURON
- Neurodegeneration in frontotemporal lobar degeneration and motor neurone disease associated with expansions inC9orf72is linked to TDP-43 pathology and not associated with aggregated forms of dipeptide repeat proteins
- (2015) Y. Davidson et al. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
- Molecular mechanisms in DM1 — a focus on foci
- (2015) Olof Joakim Pettersson et al. NUCLEIC ACIDS RESEARCH
- Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12
- (2015) Yi Dong et al. PARKINSONISM & RELATED DISORDERS
- C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficits
- (2015) J. Chew et al. SCIENCE
- RNA:DNA hybrids in the human genome have distinctive nucleotide characteristics, chromatin composition, and transcriptional relationships
- (2015) Julie Nadel et al. Epigenetics & Chromatin
- GGGGCC microsatellite RNA is neuritically localized, induces branching defects, and perturbs transport granule function
- (2015) Alondra Schweizer Burguete et al. eLife
- Dipeptide repeat protein inclusions are rare in the spinal cord and almost absent from motor neurons in C9ORF72 mutant amyotrophic lateral sclerosis and are unlikely to cause their degeneration
- (2015) Jorge Gomez-Deza et al. Acta Neuropathologica Communications
- C9ORF72 GGGGCC Expanded Repeats Produce Splicing Dysregulation which Correlates with Disease Severity in Amyotrophic Lateral Sclerosis
- (2015) Johnathan Cooper-Knock et al. PLoS One
- Sequestration of multiple RNA recognition motif-containing proteins by C9orf72 repeat expansions
- (2014) Johnathan Cooper-Knock et al. BRAIN
- Induced expression of expanded CGG RNA causes mitochondrial dysfunctionin vivo
- (2014) Renate K Hukema et al. CELL CYCLE
- Characteristic RNA foci of the abnormal hexanucleotide GGCCUG repeat expansion in spinocerebellar ataxia type 36 (Asidan)
- (2014) W. Liu et al. EUROPEAN JOURNAL OF NEUROLOGY
- RNA Granule Assembly and Disassembly Modulated by Nuclear Factor Associated with Double-stranded RNA 2 and Nuclear Factor 45
- (2014) Nobuyuki Shiina et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion
- (2014) Masato Obayashi et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Loss of MBNL Leads to Disruption of Developmentally Regulated Alternative Polyadenylation in RNA-Mediated Disease
- (2014) Ranjan Batra et al. MOLECULAR CELL
- C9orf72 nucleotide repeat structures initiate molecular cascades of disease
- (2014) Aaron R. Haeusler et al. NATURE
- The phenotypic variability of amyotrophic lateral sclerosis
- (2014) Bart Swinnen et al. Nature Reviews Neurology
- Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion
- (2014) Adrian J. Waite et al. NEUROBIOLOGY OF AGING
- Antisense Proline-Arginine RAN Dipeptides Linked to C9ORF72-ALS/FTD Form Toxic Nuclear Aggregates that Initiate In Vitro and In Vivo Neuronal Death
- (2014) Xinmei Wen et al. NEURON
- Distinctive structural motifs of RNA G-quadruplexes composed of AGG, CGG and UGG trinucleotide repeats
- (2014) Magdalena Malgowska et al. NUCLEIC ACIDS RESEARCH
- C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins
- (2014) S. Mizielinska et al. SCIENCE
- Poly-dipeptides encoded by the C9orf72 repeats bind nucleoli, impede RNA biogenesis, and kill cells
- (2014) I. Kwon et al. SCIENCE
- FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndrome
- (2014) Ronald AM Buijsen et al. Acta Neuropathologica Communications
- Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72
- (2014) Yvonne S Davidson et al. Acta Neuropathologica Communications
- The neuropathology associated with repeat expansions in the C9ORF72 gene
- (2013) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations
- (2013) Ian R. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia
- (2013) Pietro Fratta et al. ACTA NEUROPATHOLOGICA
- C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci
- (2013) Sarah Mizielinska et al. ACTA NEUROPATHOLOGICA
- Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins
- (2013) Kohji Mori et al. ACTA NEUROPATHOLOGICA
- Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS
- (2013) Tania F. Gendron et al. ACTA NEUROPATHOLOGICA
- hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations
- (2013) Kohji Mori et al. ACTA NEUROPATHOLOGICA
- Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons
- (2013) Sandra Almeida et al. ACTA NEUROPATHOLOGICA
- State of play in amyotrophic lateral sclerosis genetics
- (2013) Alan E Renton et al. NATURE NEUROSCIENCE
- Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis
- (2013) Matthew B. Harms et al. NEUROBIOLOGY OF AGING
- C9ORF72 transcription in a frontotemporal dementia case with two expanded alleles
- (2013) J. Cooper-Knock et al. NEUROLOGY
- Unconventional Translation of C9ORF72 GGGGCC Expansion Generates Insoluble Polypeptides Specific to c9FTD/ALS
- (2013) Peter E.A. Ash et al. NEURON
- RNA Toxicity from the ALS/FTD C9ORF72 Expansion Is Mitigated by Antisense Intervention
- (2013) Christopher J. Donnelly et al. NEURON
- CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome
- (2013) Peter K. Todd et al. NEURON
- Abnormal RNA structures (RNA foci) containing a penta-nucleotide repeat (UGGAA)nin the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis
- (2013) Yusuke Niimi et al. NEUROPATHOLOGY
- RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia
- (2013) T. Zu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration
- (2013) Z. Xu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration
- (2013) C. Lagier-Tourenne et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Sequestration of DROSHA and DGCR8 by Expanded CGG RNA Repeats Alters MicroRNA Processing in Fragile X-Associated Tremor/Ataxia Syndrome
- (2013) Chantal Sellier et al. Cell Reports
- Hexanucleotide Repeats in ALS/FTD Form Length-Dependent RNA Foci, Sequester RNA Binding Proteins, and Are Neurotoxic
- (2013) Youn-Bok Lee et al. Cell Reports
- The myotonic dystrophies: molecular, clinical, and therapeutic challenges
- (2012) Bjarne Udd et al. LANCET NEUROLOGY
- Clinical features of SCA36: A novel spinocerebellar ataxia with motor neuron involvement (Asidan)
- (2012) Y. Ikeda et al. NEUROLOGY
- Expansion of Intronic GGCCTG Hexanucleotide Repeat in NOP56 Causes SCA36, a Type of Spinocerebellar Ataxia Accompanied by Motor Neuron Involvement
- (2011) Hatasu Kobayashi et al. AMERICAN JOURNAL OF HUMAN GENETICS
- RNA Foci, CUGBP1, and ZNF9 Are the Primary Targets of the Mutant CUG and CCUG Repeats Expanded in Myotonic Dystrophies Type 1 and Type 2
- (2011) Karlie Jones et al. AMERICAN JOURNAL OF PATHOLOGY
- Loss of junctophilin-3 contributes to huntington disease-like 2 pathogenesis
- (2011) Ana I. Seixas et al. ANNALS OF NEUROLOGY
- Splicing factor hnRNPH drives an oncogenic splicing switch in gliomas
- (2011) Clare V LeFave et al. EMBO JOURNAL
- Mitochondrial Dysfunction and Oxidative Stress Contribute to the Pathogenesis of Spinocerebellar Ataxia Type 12 (SCA12)
- (2011) Yu-Chun Wang et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Transgenic mice with SCA10 pentanucleotide repeats show motor phenotype and susceptibility to seizure: A toxic RNA gain-of-function model
- (2011) Misti White et al. JOURNAL OF NEUROSCIENCE RESEARCH
- A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
- (2011) Ilse Gijselinck et al. LANCET NEUROLOGY
- Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy
- (2011) Charlotte Fugier et al. NATURE MEDICINE
- An Antisense CAG Repeat Transcript at JPH3 Locus Mediates Expanded Polyglutamine Protein Toxicity in Huntington's Disease-like 2 Mice
- (2011) Brian Wilburn et al. NEURON
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
- (2011) Mariely DeJesus-Hernandez et al. NEURON
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
- (2011) Alan E. Renton et al. NEURON
- Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients
- (2010) Chantal Sellier et al. EMBO JOURNAL
- Expansion of CUG RNA repeats causes stress and inhibition of translation in myotonic dystrophy 1 (DM1) cells
- (2010) Claudia Huichalaf et al. FASEB JOURNAL
- CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1
- (2010) Amanda J. Ward et al. HUMAN MOLECULAR GENETICS
- Dysregulation and cellular mislocalization of specific miRNAs in myotonic dystrophy type 1
- (2010) Riccardo Perbellini et al. NEUROMUSCULAR DISORDERS
- Non-ATG-initiated translation directed by microsatellite expansions
- (2010) T. Zu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Histone Deacetylases Suppress CGG Repeat–Induced Neurodegeneration Via Transcriptional Silencing in Models of Fragile X Tremor Ataxia Syndrome
- (2010) Peter K. Todd et al. PLoS Genetics
- Inactivation of hnRNP K by Expanded Intronic AUUCU Repeat Induces Apoptosis Via Translocation of PKCδ to Mitochondria in Spinocerebellar Ataxia 10
- (2010) Misti C. White et al. PLoS Genetics
- Spinocerebellar Ataxia Type 31 Is Associated with “Inserted” Penta-Nucleotide Repeats Containing (TGGAA)n
- (2009) Nozomu Sato et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Expression of RNA CCUG Repeats Dysregulates Translation and Degradation of Proteins in Myotonic Dystrophy 2 Patients
- (2009) Elizabeth Salisbury et al. AMERICAN JOURNAL OF PATHOLOGY
- Evidence against haploinsuffiency of human ataxin 10 as a cause of spinocerebellar ataxia type 10
- (2009) Boris Keren et al. NEUROGENETICS
- RNA Gain-of-Function in Spinocerebellar Ataxia Type 8
- (2009) Randy S. Daughters et al. PLoS Genetics
- Muscleblind-like 2 (Mbnl2) -deficient mice as a model for myotonic dystrophy
- (2008) Minqi Hao et al. DEVELOPMENTAL DYNAMICS
- A Comparison of Huntington Disease and Huntington Disease-Like 2 Neuropathology
- (2008) Dobrila D. Rudnicki et al. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
- MBNL1 associates with YB-1 in cytoplasmic stress granules
- (2008) Hayato Onishi et al. JOURNAL OF NEUROSCIENCE RESEARCH
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started